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71.
袁欣欣 《数学的实践与认识》2009,39(13)
以四连杆机械为例,其自由度是1,整个机构的质心只需一个独立参变数描述.故机构的质心对该参数的导数等于零即机构质量中心保持固定的充要条件.通过对线性方程组基础理论的巧妙利用,给出了四连杆在工作状态下质心保持稳定的几何特征. 相似文献
72.
With the development of information technology, it has become a popular topic to share data from multiple sources without privacy disclosure problems. Privacy-preserving record linkage (PPRL) can link the data that truly matches and does not disclose personal information. In the existing studies, the techniques of PPRL have mostly been studied based on the alphabetic language, which is much different from the Chinese language environment. In this paper, Chinese characters (identification fields in record pairs) are encoded into strings composed of letters and numbers by using the SoundShape code according to their shapes and pronunciations. Then, the SoundShape codes are encrypted by Bloom filter, and the similarity of encrypted fields is calculated by Dice similarity. In this method, the false positive rate of Bloom filter and different proportions of sound code and shape code are considered. Finally, we performed the above methods on the synthetic datasets, and compared the precision, recall, F1-score and computational time with different values of false positive rate and proportion. The results showed that our method for PPRL in Chinese language environment improved the quality of the classification results and outperformed others with a relatively low additional cost of computation. 相似文献
73.
Hao Gao Yongqing Wang Jiangli Shao Huawei Shen Xueqi Cheng 《Entropy (Basel, Switzerland)》2022,24(11)
Users participate in multiple social networks for different services. User identity linkage aims to predict whether users across different social networks refer to the same person, and it has received significant attention for downstream tasks such as recommendation and user profiling. Recently, researchers proposed measuring the relevance of user-generated content to predict identity linkages of users. However, there are two challenging problems with existing content-based methods: first, barely considering the word similarities of texts is insufficient where the semantical correlations of named entities in the texts are ignored; second, most methods use time discretization technology, where the texts are divided into different time slices, resulting in failure of relevance modeling. To address these issues, we propose a user identity linkage model with the enhancement of a knowledge graph and continuous time decay functions that are designed for mitigating the influence of time discretization. Apart from modeling the correlations of the words, we extract the named entities in the texts and link them into the knowledge graph to capture the correlations of named entities. The semantics of texts are enhanced through the external knowledge of the named entities in the knowledge graph, and the similarity discrimination of the texts is also improved. Furthermore, we propose continuous time decay functions to capture the closeness of the posting time of texts instead of time discretization to avoid the matching error of texts. We conduct experiments on two real public datasets, and the experimental results show that the proposed method outperforms state-of-the-art methods. 相似文献
74.
The Challenge of Deciphering Linkage Isomers in Mixtures of Oligomeric Complexes Derived from 9‐Methyladenine and trans‐(NH3)2PtII Units
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Dr. Susana Ibáñez Dr. Béla Mihály Dr. Pablo J. Sanz Miguel Prof. Dr. Dirk Steinborn Irene Pretzer Dr. Wolf Hiller Prof. Dr. Bernhard Lippert 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(15):5794-5806
Metal coordination to N9‐substituted adenines, such as the model nucleobase 9‐methyladenine (9MeA), under neutral or weakly acidic pH conditions in water preferably occurs at N1 and/or N7. This leads, not only to mononuclear linkage isomers with N1 or N7 binding, but also to species that involve both N1 and N7 metal binding in the form of dinuclear or oligomeric species. Application of a trans‐(NH3)2PtII unit and restriction of metal coordination to the N1 and N7 sites and the size of the oligomer to four metal entities generates over 50 possible isomers, which display different feasible connectivities. Slowly interconverting rotamers are not included in this number. Based on 1H NMR spectroscopic analysis, a qualitative assessment of the spectroscopic features of N1,N7‐bridged species was attempted. By studying the solution behavior of selected isolated and structurally characterized compounds, such as trans‐[PtCl(9MeA‐N7)(NH3)2]ClO4 ? 2H2O or trans,trans‐[{PtCl(NH3)2}2(9MeA‐N1,N7)][ClO4]2 ? H2O, and also by application of a 9MeA complex with an (NH3)3PtII entity at N7, [Pt(9MeA‐N7)(NH3)3][NO3]2, which blocks further cross‐link formation at the N7 site, basic NMR spectroscopic signatures of N1,N7‐bridged PtII complexes were identified. Among others, the trinuclear complex trans‐[Pt(NH3)2{μ‐(N1‐9MeA‐N7)Pt(NH3)3}2][ClO4]6 ? 2H2O was crystallized and its rotational isomerism in aqueous solution was studied by NMR spectroscopy and DFT calculations. Interestingly, simultaneous PtII coordination to N1 and N7 acidifies the exocyclic amino group of the two 9MeA ligands sufficiently to permit replacement of one proton each by a bridging heterometal ion, HgII or CuII, under mild conditions in water. 相似文献
75.
Scott Nollet 《Transactions of the American Mathematical Society》1996,348(3):1137-1162
In this paper we generalize the and -type resolutions used by Martin-Deschamps and Perrin for curves in to subschemes of pure codimension in projective space, and shows that these resolutions are interchanged by the mapping cone procedure under a simple linkage. Via these resolutions, Rao's correspondence is extended to give a bijection between even linkage classes of subschemes of pure codimension two and stable equivalence classes of reflexive sheaves satisfying and . Further, these resolutions are used to extend the work of Martin-Deschamps and Perrin for Cohen-Macaulay curves in to subschemes of pure codimension two in . In particular, even linkage classes of such subschemes satisfy the Lazarsfeld-Rao property and any minimal subscheme for an even linkage class links directly to a minimal subscheme for the dual class.
76.
77.
Functionalisation of calix[4]arene at both the wide and narrow rims leads to the formation of compounds containing bipyridyl, via an amide linkage, at the wide rim and having either a butyl chain, a benzyl group or an alkyl ester functionality at the narrow rim. All compounds were characterised using 1H and 13C NMR spectroscopies. Initial binding studies with Ru(bipy)2Cl2 are reported. 相似文献
78.
Atsushi Kaji Yosikazu Arimatsu Masao Murano 《Journal of polymer science. Part A, Polymer chemistry》1992,30(2):287-297
Several kinds of model compounds for anomalous linkages in polyurethanes (branching or crosslinking; allophanate and biuret) were prepared. The phenylisocyanate (PHI) based models were identified by IR and NMR. The 13C-NMR chemical shifts effects due to the anomalous linkages were determined. The 4,4′-diphenylmethane diisocyanate (MDI) based models were purified incompletely but the characteristic signals of the aromatic carbons were nevertheless found in their spectra. Two types of segmented polyurethane (SPU) were prepared and the anomalous linkages were investigated by 13C-NMR. The signals due to the allophanate (Al) and the triphenylbiuret (TB) linkages were observed in the spectra of the SPU prepared at high temperature (>80°C) or prepolymer gels yielded by abnormal reaction. A small signal due to a phenyl carbon of biuret (Bi) linkage was observed even in a normally prepared SPU (polyetherurethane-urea). Employing the phenyl carbon signals was advantageous for the determination of anomalous linkages because of their larger intensities. 相似文献
79.
A method for analysing sialyl oligosaccharides from bovine colostrum using high-performance liquid chromatography-electrospray ionisation-mass spectrometry (HPLC-ESI-MS) is described. Under positive ionisation mode, mass spectra of alpha2-3 and alpha2-6 linkages were different, and the former produced a prominent B2 (or B3 in disialyl lactose) mass fragment. This fragment was absent from mass spectra with alpha2-6 linkages. Two sialyl oligosaccharides, which have not been reported previously, were tentatively identified. One comprises a N-acetyl neuraminic acid (Neu5Ac), two hexoses (Hex), and one N-acetyl hexosamine (HexNAc) residue ((Neu5Ac)1 (Hex)2 (HexNAc)1), and the other comprises one Neu5Ac and one Hex residue ((Neu5Ac)1(Hex)1). 相似文献
80.
Saravanan Raju Ray J. Butcher Harkesh B. Singh 《Acta Crystallographica. Section C, Structural Chemistry》2019,75(3):336-341
The structures of the 18‐membered diselenide‐linked macrocycle 10,27‐di‐tert‐butyl 11,28‐dioxo‐2,3,19,20‐tetraselena‐10,12,27,29‐tetraazapentacyclo[28.4.0.04,9.013,18.021,26]tetratriaconta‐1(30),4(9),5,7,13,15,17,21,23,25,31,33‐dodecaene‐10,27‐dicarboxylate, C36H34N4O6Se4, and its precursor di‐tert‐butyl 2,2′‐[diselane‐1,2‐diylbis(2,1‐phenylene)]dicarbamate, C22H28N2O4Se2, are reported. The precusor to the macrocycle contains two tert‐butyl phenylcarbamate arms connected to a diselenide group, with Se—C and Se—Se bond lengths of 1.914 (4) and 2.3408 (6) Å, respectively. The macrocycle resides on a crystallographic center of inversion in space group P with one molecule in the unit cell (Z′ = ). It contains an 18‐membered macrocyclic ring with two diselenide linkages. In this macrocycle, there are two free and two protected amino groups. 相似文献